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Víctor Romero-Rochín

Publications and source records attributed to Víctor Romero-Rochín.

5 recordsLinked to original sources

Interfacial properties of liquid-vapor interfaces with planar, spherical, and cylindrical geometries in mean field.

Following the route of the stress tensor we study the free energy of a fluid liquid-vapor interface in the van der Waals approximation for planar, cylindrical and spherical interfaces. By performing a systematic expansion in powers of the inverse of the curvature radii, and appropriately defining the Gibbs dividing surface, we find unambiguous expressions for the surface tension, the spontaneous curvature, the bending rigidity and the Gaussian rigidity.

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Thermodynamics and phase transitions in a fluid confined by a harmonic trap.

We study a fluid of interacting atoms confined by a three-dimensional anisotropic harmonic potential, similar to those produced by the magnetic traps used to confine cold atoms. We show that instead of the usual thermodynamic variables pressure and volume, no longer existing in this case, there appear "new" variables: the volume is replaced by (the inverse cube of) the geometric average of the oscillator frequencies of the trap, and the hydrostatic pressure is replaced by an intensive variable, conjugate to the previous one, and responsible for the mechanical equilibrium of the fluid in the trap. We discuss the origin and physical meaning of these new variables. With the aid of molecular dynamics simulations we show the emergence of novel liquid, vapor and solid-like phases in a classical fluid. In particular, we calculate the liquid-vapor-like coexistence curve and show evidence for the appearance of a critical point. These phase transitions should be observable in fluids of not-so-cold alkaline atoms.

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Equation of state of an interacting bose gas confined by a harmonic trap: the role of the "harmonic" pressure.

A gas of interacting atoms confined by a three dimensional anisotropic harmonic potential is studied. It is shown that there appear "new" thermodynamic variables instead of the usual pressure and volume: the latter is replaced by (the inverse of) the cube of the geometric average of the oscillator frequencies of the trap, and the former by the harmonic pressure responsible for the mechanical equilibrium of the fluid in the trap. We discuss the origin and physical meaning of these quantities and show that the equation of state of the gas is given in terms of these variables. The equation of state of a cold gas of interacting Bose atoms in the Hartree-Fock approximation is presented. We indicate how the harmonic pressure can be measured in current experiments.

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Molecular wave packet interferometry and quantum entanglement.

We study wave packet interferometry (WPI) considering the laser pulse fields both classical and quantum mechanically. WPI occurs in a molecule after subjecting it to the interaction with a sequence of phase-locked ultrashort laser pulses. Typically, the measured quantity is the fluorescence of the molecule from an excited electronic state. This signal has imprinted the interference of the vibrational wave packets prepared by the different laser pulses of the sequence. The consideration of the pulses as quantum entities in the analysis allows us to study the entanglement of the laser pulse states with the molecular states. With a simple model for the molecular system, plus several justified approximations, we solve for the fully quantum mechanical molecule-electromagnetic field state. We then study the reduced density matrices of the molecule and the laser pulses separately. We calculate measurable corrections to the case where the fields are treated classically.

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Preparation and resolution of molecular states by coherent sequences of phase-locked ultrashort laser pulses.

We study the application of nonlinear wave packet interferometry to the preparation and resolution of the overlaps of nonstationary nuclear wave functions evolving in an excited electronic state of a diatomic molecule. It is shown that possible experiments with two phase-locked ultrashort pulsepairs can be used to determine a specific vibrational wave packet state in terms of coherent states of the ground electronic state. We apply this scheme to an idealized molecule with harmonic potential energy surfaces and to the X <-- B transition states of the iodine molecule. Our results indicate that this scheme is very promising as a potential tool to quantum control.

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